His primary areas of investigation include Genetics, Mutation, Molecular biology, Gene and Pathology. He integrates many fields, such as Genetics and MICROCEPHALIN, in his works. The concepts of his Molecular biology study are interwoven with issues in Vimentin, Apoptosis, Macrophage migration inhibitory factor and Adenomatous polyposis coli.
His Adenomatous polyposis coli study integrates concerns from other disciplines, such as Stromal cell, Angiogenesis, Intestinal mucosa, Cytokine and Colorectal adenoma. In the subject of general Gene, his work in Familial exudative vitreoretinopathy, Genetic screen and Stop codon is often linked to TSPAN12 and FZD4, thereby combining diverse domains of study. His work deals with themes such as Carcinogenesis, Internal medicine and Immunofluorescence, which intersect with Pathology.
Alexander F. Markham mostly deals with Genetics, Gene, Molecular biology, Locus and Mutation. His study in Gene mapping, Exon, Genome, Sequence analysis and DNA sequencing falls within the category of Genetics. His biological study spans a wide range of topics, including Cancer research and Virology.
Alexander F. Markham has included themes like Biochemistry, DNA, DNA repair, Point mutation and Complementary DNA in his Molecular biology study. In most of his Locus studies, his work intersects topics such as Haplotype. His research on Mutation often connects related areas such as Internal medicine.
His scientific interests lie mostly in Genetics, Nanotechnology, Computational biology, In vivo and Exome sequencing. He connects Genetics with TSPAN12 in his study. His work on Surface plasmon resonance and Nanomaterials as part of his general Nanotechnology study is frequently connected to Fabrication and Particle, thereby bridging the divide between different branches of science.
His study on Computational biology also encompasses disciplines like
Alexander F. Markham spends much of his time researching Genetics, Nanotechnology, Exome sequencing, Preclinical imaging and Fabrication. His study deals with a combination of Genetics and Ciliary Motility Disorders. His Nanotechnology research incorporates elements of Crystallinity and Biodistribution.
His studies in Exome sequencing integrate themes in fields like Molecular genetics, Consanguinity, Ubiquitin ligase and Massive parallel sequencing. His Nanomaterials research integrates issues from Nanofiber, One-Step, Bifunctional and Nanostructure. His Exome study combines topics from a wide range of disciplines, such as Disease gene identification, Genome, Genotyping, Genotype and Sequence analysis.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
ASPM is a major determinant of cerebral cortical size.
Jacquelyn Bond;Emma Roberts;Ganesh H. Mochida;Ganesh H. Mochida;Daniel J. Hampshire.
Nature Genetics (2002)
Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain
Andrew P. Jackson;Andrew P. Jackson;Helen Eastwood;Sandra M. Bell;Jimi Adu.
American Journal of Human Genetics (2002)
EB1, a protein which interacts with the APC tumour suppressor, is associated with the microtubule cytoskeleton throughout the cell cycle.
E E Morrison;B N Wardleworth;J M Askham;A F Markham.
Oncogene (1998)
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
Arthur B. McKie;John C. McHale;T. Jeffrey Keen;Emma E. Tarttelin.
Human Molecular Genetics (2001)
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
Sandeep Uppal;Sandeep Uppal;Christine P Diggle;Ian M Carr;Colin W G Fishwick.
Nature Genetics (2008)
Localization of cyclooxygenase-2 in human sporadic colorectal adenomas.
Keith S. Chapple;Elizabeth J. Cartwright;Gillian Hawcroft;Alison Tisbury.
American Journal of Pathology (2000)
Reduced expression of oestrogen receptor beta in invasive breast cancer and its re-expression using DNA methyl transferase inhibitors in a cell line model.
George P Skliris;Kailas Munot;Kailas Munot;Sandra M Bell;Pauline J Carder.
The Journal of Pathology (2003)
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.
Carmel Toomes;Nicola J. Marchbank;David A. Mackey;Jamie E. Craig.
Human Molecular Genetics (2001)
Dysregulated lymphocyte proliferation and differentiation in patients with rheumatoid arthritis
Frederique Ponchel;Ann W. Morgan;Sarah J. Bingham;Mark Quinn.
Blood (2002)
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
James A. Poulter;Manir Ali;David F. Gilmour;Aine Rice.
American Journal of Human Genetics (2010)
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